Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Sep:220:107355.
doi: 10.1016/j.clineuro.2022.107355. Epub 2022 Jun 27.

Calcitonin gene-related peptide and neurologic injury: An emerging target for headache management

Affiliations
Review

Calcitonin gene-related peptide and neurologic injury: An emerging target for headache management

Yusuf Mehkri et al. Clin Neurol Neurosurg. 2022 Sep.

Abstract

Calcitonin gene-related peptide (CGRP) is a 37-amino acid neuropeptide known to be involved in the trigeminovascular system and to function as a potent vasodilator. Although it has emerged as a viable target for headache management with targeted treatments developed for migraine, a highly disabling neurovascular disorder, less is known about CGRP's role in other neurologic conditions such as traumatic brain injury and subarachnoid hemorrhage. The literature has shown that during these injury cascades, CGRP receptors are modulated in varying ways. Therefore, CGRP or its receptors might be viable targets to manage secondary injuries following acute brain injury. In this review, we highlight the pathophysiology of the CGRP pathway and its relation to migraine pathogenesis. Using these same principles, we assess the existing preclinical data for CGRP and its role in acute brain injury. The findings are promising, and set the basis for further work, with specific focus on the therapeutic benefit of CGRP modulation following neurologic injury.

Keywords: Calcitonin gene-related peptide; Headache; Subarachnoid hemorrhage; Traumatic brain injury; Treatment approaches.

PubMed Disclaimer

MeSH terms

Substances